Study Characteristics for Randomized Controlled Trials included in the NCPTSD's PTSD Repository.

Values reported as "NA" or not reported "NR" by the study are null values (empty cells).

The Study Interventions dataset includes information about each of 861 specific treatment arms that were studied in all 389 RCTs. Each study arm was coded to indicate the type of intervention or comparison condition. This dataset includes the study-level Study Class as well as individual variables for each category of treatment, coded as Yes or No for each arm. Study arm treatment category variables are as follows: Pharmacotherapy (as well as a subclass such as antidepressant, antianxiety, etc.); Psychotherapy (as well as a subclass to identify trauma-focused or non-trauma-focused therapy); Complementary and Integrative Health (CIH; as well as a subclass such as relaxation or meditation); Nonpharmacologic Biological; Nonpharmacologic Cognitive; Collaborative Care; Other Treatments; Control

The Study Intervention dataset also includes information on the format of the treatment (individual, group, couples, mixed); treatment delivery method (in person, by phone, by video, technology alone, technology assisted, written or mixed); dose or amount of treatment and, treatment completion and adherence. Use this dataset to learn about treatment studies of a particular type

Each record is an arm of the study, labeled as A, B, C, or D. Values abstracted as not applicable ("NA") or not reported ("NR") from the study are null values (empty cells).

Sample Characteristics for Randomized Controlled Trials included in the NCPTSD's PTSD Repository.

Values reported as "NA" or not reported "NR" by the study are null values (empty cells).

Study Interventions for randomized controlled trials included in the NCPTSD's PTSD Repository.

Each record is an arm of the study, labeled as A, B, C, or D.

Values abstracted as not applicable ("NA") or not reported ("NR") from the study are null values (empty cells).

Population Characteristics for Randomized Controlled Trials included in the NCPTSD's PTSD Repository.

Values reported as "NA" or not reported "NR" by the study are null values (empty cells).

Study Interventions for randomized controlled trials included in the NCPTSD's PTSD-Repository.

Each record is an arm of the study, labeled as A, B, C, or D.

Values abstracted as not applicable ("NA") or not reported ("NR") from the study are null values (empty cells).

The Study Interventions dataset includes information about each of 861 specific treatment arms that were studied in all 389 RCTs. Each study arm was coded to indicate the type of intervention or comparison condition. This dataset includes the study-level Study Class as well as individual variables for each category of treatment, coded as Yes or No for each arm. Study arm treatment category variables are as follows: Pharmacotherapy (as well as a subclass such as antidepressant, antianxiety, etc.); Psychotherapy (as well as a subclass to identify trauma-focused or non-trauma-focused therapy); Complementary and Integrative Health (CIH; as well as a subclass such as relaxation or meditation); Nonpharmacologic Biological; Nonpharmacologic Cognitive; Collaborative Care; Other Treatments; Control

The Study Intervention dataset also includes information on the format of the treatment (individual, group, couples, mixed); treatment delivery method (in person, by phone, by video, technology alone, technology assisted, written or mixed); dose or amount of treatment and, treatment completion and adherence. Use this dataset to learn about treatment studies of a particular type

Each record is an arm of the study, labeled as A, B, C, or D. Values abstracted as not applicable ("NA") or not reported ("NR") from the study are null values (empty cells).

Study Interventions for randomized controlled trials included in the NCPTSD's PTSD-Repository.

Each record is an arm of the study, labeled as A, B, C, or D.

Values abstracted as not applicable ("NA") or not reported ("NR") from the study are null values (empty cells).

Risk of Bias Assessment

Risk of Bias (ROB) assessment was conducted for all included studies following the framework established in Comparative Effectiveness Review (CER) No. 207, which is based on the Agency for Healthcare Research and Quality (AHRQ) Methods Guide for Comparative Effectiveness Reviews with an added question on whether authors reported all prespecified outcomes (assessing reporting bias).